Description

Clips read alignments where they match BED file defined regions

Input

name:type
description
pattern

meta

:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

bam

:file

BAM/CRAM/SAM file

*.{bam,cram,sam}

bed

:file

BED file of regions to be removed (e.g. amplicon primers)

*.{bed}

save_cliprejects

:boolean

Save filtered reads to a file

save_clipstats

:boolean

Save clipping stats to a file

Output

name:type
description
pattern

bam

meta

:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

*.clipallowed.bam

:file

Clipped reads BAM file

*.{bam}

stats

meta

:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

*.clipstats.txt

:file

Clipping statistics text file

*.{clipstats.txt}

rejects_bam

meta

:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

*.cliprejects.bam

:file

Filtered reads BAM file

*.{cliprejects.bam}

versions_samtools

${task.process}

:string

The name of the process

samtools

:string

The name of the tool

samtools version | sed '1!d;s/.* //'

:eval

The expression to obtain the version of the tool

Topics

name:type
description
pattern

versions

${task.process}

:string

The name of the process

samtools

:string

The name of the tool

samtools version | sed '1!d;s/.* //'

:eval

The expression to obtain the version of the tool

Tools

samtools
MIT

SAMtools is a set of utilities for interacting with and post-processing short DNA sequence read alignments in the SAM, BAM and CRAM formats, written by Heng Li. These files are generated as output by short read aligners like BWA.